OMOP Concept 376938
Neurofibromatosis syndrome
StandardConditionSNOMED19133005Disorder
Maps from
17
Descendants
17
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
17 source codes normalize to Neurofibromatosis syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 115280 | Neurofibromatosis | Non-standard |
| CIEL | 133107 | Neurofibromatosis, type 3 | Non-standard |
| CIM10 | Q85.0 | Neurofibromatosis (nonmalignant) | Non-standard |
| ICD10 | Q85.0 | Neurofibromatosis (nonmalignant) | Non-standard |
| ICD10CM | Q85.0 | Neurofibromatosis (nonmalignant) | Non-standard |
| ICD10CM | Q85.00 | Neurofibromatosis, unspecified | Non-standard |
| ICD10CM | Q85.09 | Other neurofibromatosis | Non-standard |
| ICD10CN | Q85.0 | Neurofibromatosis (nonmalignant) | Non-standard |
| ICD10CN | Q85.000 | Neurofibromatosis (nonmalignant) | Non-standard |
| ICD10CN | Q85.001 | Von Recklinghausen's disease (machine translation) | Non-standard |
| ICD10GM | Q85.0 | Neurofibromatosis (nonmalignant) | Non-standard |
| ICD9CM | 237.7 | Neurofibromatosis | Non-standard |
| ICD9CM | 237.70 | Neurofibromatosis, unspecified | Non-standard |
| ICD9CM | 237.79 | Other neurofibromatosis | Non-standard |
| KCD7 | Q85.0 | Neurofibromatosis (nonmalignant) | Non-standard |
| MeSH | D017253 | Neurofibromatoses | Non-standard |
| Nebraska Lexicon | 19133005 | Clinical neurofibromatosis | Non-standard |
Synonyms
Alternative names recorded for Neurofibromatosis syndrome across source vocabularies.
- Clinical neurofibromatosis
- neurofibromatosis clínica
- Neurofibromatosis syndrome (disorder)
- NF - Neurofibromatosis
- síndrome de neurofibromatosis
- síndrome de neurofibromatosis (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(38)Roll up to these when you need a wider cohort.
- 1Neoplasm of nerve sheath origin
- 1Neoplasm of uncertain behavior of nervous system
- 1Neoplasm of uncertain behavior of skin
- 1Neurocutaneous syndrome
- 1Skin tumor of neural origin
- 2Congenital disease
- 2Disorder involving the integument of fetus OR newborn
- 2Neoplasm of nervous system
- 2Neoplasm of skin
- 2Neoplasm of uncertain behavior of soft tissues
- 2Neoplastic disease
- 2Neoplastic disease of uncertain behavior
- 3Disorder of fetus and/or newborn
- 3Disorder of integument
- 3Disorder of nervous system
- 3Mass of skin
- 3Neoplasm and/or hamartoma
- 3Neoplasm of integumentary system
- 3Neoplasm of soft tissue
- 3Skin lesion
- 3Space-occupying lesion of nervous system
- 4Disease
- 4Disorder of body system
- 4Disorder of skin
- 4Integumentary system finding
Narrower concepts
(17)Included automatically when you query with descendants.
- 1Café-au-lait macules with pulmonary stenosis
- 1Café-au-lait macules with temporal dysrhythmia
- 1Exacerbation of neurofibromatosis syndrome
- 1Full schwannomatosis
- 1Neurofibromatosis type 1
- 1Neurofibromatosis type 2
- 1Segmental neurofibromatosis
- 217q11 deletion syndrome
- 2Axillary freckling due to neurofibromatosis
- 2Elephantiasis neurofibromatosa
- 2Familial spinal neurofibromatosis
- 2Mosaic neurofibromatosis type 1
- 2Mosaic neurofibromatosis type 2
- 2Multiple café-au-lait macules due to neurofibromatosis
- 2Multiple neurofibromas in neurofibromatosis
- 2Neurofibromatosis Noonan syndrome
- 2Segmental neurofibromatosis type 1
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